Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,060 recalls have been distributed to Missouri in the last 12 months.
Showing 14261–14280 of 52,570 recalls
Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...
The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a software issue associated with the ability to properly complete a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cantharidin PLUS Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl/Epinephrine Recalled by Edge Pharma, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLT Topical Cream Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl/Tropicamide Recalled by Edge Pharma, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dibutyl Squaric Acid Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dibutyl Squaric Acid Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Profound Dental Gel Recalled by Edge Pharma, LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone sodium phosphate 0.4% Recalled by Edge Pharma, LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.